A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957814



Internal ID15905084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:809239..1385941hg38UCSC Ensembl
Innerchr3:850922..1427625hg19UCSC Ensembl
Innerchr3:825922..1402625hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38576703
hg19576704
hg18576704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589306
Supporting Variants
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957814
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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